Darbepoetin alfa administration in patients with non-Hodgkin lymphoma and chemotherapy-induced anemia receiving (±R)CHOP

التفاصيل البيبلوغرافية
العنوان: Darbepoetin alfa administration in patients with non-Hodgkin lymphoma and chemotherapy-induced anemia receiving (±R)CHOP
المؤلفون: Matthias Schwenkglenks, Ruth Pettengell, Corinne Haioun, Francesca Gaia Rossi, Pieternella J. Lugtenburg, Ulrich Duehrsen, B. Pujol, Antonio Salar Silvestre, Tracey Wheeler, Gregor Verhoef
المساهمون: University of Zurich, Pettengell, Ruth
المصدر: Hematology. 18:26-29
بيانات النشر: Informa UK Limited, 2013.
سنة النشر: 2013
مصطلحات موضوعية: Male, medicine.medical_specialty, Vincristine, Cyclophosphamide, Darbepoetin alfa, Anemia, Prednisolone, medicine.medical_treatment, 2720 Hematology, Medizin, 610 Medicine & health, CHOP, Gastroenterology, Drug Administration Schedule, Antibodies, Monoclonal, Murine-Derived, Internal medicine, Antineoplastic Combined Chemotherapy Protocols, medicine, Humans, Erythropoietin, Chemotherapy, business.industry, Lymphoma, Non-Hodgkin, 10060 Epidemiology, Biostatistics and Prevention Institute (EBPI), Hematology, Middle Aged, medicine.disease, Treatment Outcome, Doxorubicin, Immunology, Hematinics, Female, Rituximab, business, medicine.drug
الوصف: IMPACT NHL was a multicenter, observational study in adults with non-Hodgkin lymphoma receiving CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) chemotherapy with or without rituximab. Erythropoietin-stimulating agent treatment was given according to routine clinical practice and physician preference. In a subanalysis, outcomes were evaluated in 207 patients who received darbepoetin alfa (DA). The most common reason (81%) for initiating DA was low/declining hemoglobin (Hb) concentration. Mean (±standard deviation) duration of DA exposure was 8.8 ± 6.9 weeks (mean number of doses, 5.1 ± 4.6). Overall, 23% of patients had chemotherapy and DA treatment synchronized more than 75% of the time. At the time of DA initiation, 67% of patients had Hb concentrations in the guideline-recommended range (9-11 g/dl). Of 89 patients with Hb concentrations10 g/dl at DA initiation and still receiving DA 5 weeks later, 92% (Kaplan-Meier) achieved Hb concentrations 10-12 g/dl between week 5 and at the end of treatment.
وصف الملف: 69454.pdf - application/pdf
تدمد: 1607-8454
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4e33caa538992d6d6167dbcc5ba17a5
https://doi.org/10.1179/1607845412y.0000000033
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....d4e33caa538992d6d6167dbcc5ba17a5
قاعدة البيانات: OpenAIRE